RegWardenFDA facility compliance records
Facility

The Brewer Company LLC

1 recall(s) on record — most severe on record: Class II.

Activity by year

FDA actions on record by year2018: 1 recalls; 2025: 1 inspections201712018201920202021202220232024120252026
  • Recalls (1)
  • Inspections (1)

Devices registered here (1)

  • Mattress, Flotation Therapy, Non-Powered
    Product code IKY (opens in a new tab) · Class I · General Hospital · 21 CFR 880.5150

Recalls & enforcement

  • Class IITerminated2018-03-29
    One lot, the wire harness was over-crimped on some of the connectors that go to the two vertical side switches on the exam table.

FDA inspections (1)

  • NAI2025-05-22
    No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

Related

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “The Brewer Company LLC (FEI 2182536) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/2182536-the-brewer-company-llc/

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